Ambien
Product Images NDC 0024-5521

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ambien (NDC 0024-5521). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sanofi-aventis U.s. Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Chemical Structure (Ambien Cr 01)

Chemical structure diagram showing molecular structures, likely representing the active ingredients related to Ambien CR. The image includes a complex multi-ring structure and a smaller molecular group with hydroxyl and carboxyl groups.*

FDA Label Image

Figure 1 (Ambien Cr 02)

A pharmacokinetic graph comparing zolpidem plasma concentrations (ng/mL) over time (hours) between 12.5 mg Ambien CR and 10 mg zolpidem tartrate immediate release. The chart displays concentration curves, with Ambien CR showing a more sustained plasma level over 8 hours than the immediate release form.*

FDA Label Image

Principal Display Panel (6.25 mg Tablet Bottle Label)

Label for Ambien CR 6.25 mg extended-release tablets. The label indicates a 100 tablet count, prescription only, manufactured by Sanofi-Aventis U.S. LLC. Includes storage instructions, a barcode, NDC 0024-5501-31, and mentions dispensing with a Medication Guide.*

FDA Label Image

Principal Display Panel (12.5 mg Tablet Bottle Label)

Label for Ambien CR 12.5 mg extended-release tablets by Sanofi-Aventis U.S. LLC. The label states 'Dispense with Medication Guide' with a package quantity of 100 tablets. It includes storage instructions, barcode, and regulatory information along with the NDC number 0024-5521-31.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.